Development of eco-friendly antifungal and antibacterial adhesive derived from modified cassava starch waste/polyvinyl alcohol containing green synthesized nano-silver.

Environmentally friendly biopolymer-based wood adhesives are an inevitable trend of wood product development to replace the use of harmful formaldehyde-based adhesives. In this research, a new eco-friendly modified cassava starch waste-based adhesive via carboxymethylation (CMS), and blending with polyvinyl alcohol (PVA), tannic acid (TA) and green synthesized silver nanoparticles (AgNPs) was prepared. The effects of TA content on green synthesis of AgNPs (Ag-TA) and bio-adhesive nanocomposite properties were investigated. The use of 5 wt% TA for AgNPs synthesis (Ag-TA-5) resulted in a uniform particle size distribution. The plywood prepared with Ag-TA-5 provided the highest dry and wet shear strength at 1.95 ± 0.11 MPa and 1.38 ± 0.3 MPa, respectively. The water absorption and thickness swelling of this plywood remarkably decreased up to 10.99% and 6.79%, respectively. More importantly, the presence of Ag-TA in CMS/PVA adhesive successfully inhibited the invasion of mold and bacteria. Based on the cyclic delamination test, the adhesive bond durability of bio-adhesive containing Ag-TA-5 could meet the requirement of the AITC Test T110-2007 and was comparable to commercial adhesives. The added advantage of the prepared bio-adhesive was its synthesis from agro-waste products and possible economically viable production at industrial level.

Tailoring the phosphorus release from biochar-based fertilizers: role of magnesium or calcium addition during co-pyrolysis.

The presence of magnesium (Mg) and calcium (Ca) in biochar-based fertilizers is linked to the slow release of phosphorus (P), but these alkali metals have not been systematically compared under identical conditions. In this study, sugarcane filter cake was treated with H3PO4 and MgO or CaO followed by pyrolysis at 600 °C to produce a Mg/P-rich biochar (MgPA-BC) and a Ca/P-rich biochar (CaPA-BC), respectively. The P-loaded biochars were studied by extraction and kinetic release in water over 240 hours to assess the potential P availability. X-ray diffraction and Fourier-transform infrared (FTIR) spectroscopy were used to characterize the pristine and post-kinetics biochars to identify the responsible phases for phosphate release. Additionally, the dissolved P concentrations in the kinetic release experiment were compared to thermodynamic solubility calculations of common Mg and Ca phosphates. Both MgPA-BC and CaPA-BC had P loadings of 73-74 g kg-1 but showed distinctly different release behaviors. Phosphate dissolution from MgPA-BC was gradual and reached 10 g P per kg biochar after 240 hours, with rate-determining phases being Mg2P2O7 (Mg pyrophosphate), MgNH4PO4·6H2O (struvite), and Mg3(PO4)2·22H2O (cattiite). In contrast, CaPA-BC only released 1.2 g P per kg biochar. Phosphate release from CaPA-BC was limited by the low solubility of Ca2P2O7 (Ca pyrophosphate) and (Ca,Mg)3(PO4)2 (whitlockite). Co-pyrolysis with MgO retained P in a more soluble and available form than CaO, making MgO a preferential additive over CaO to immobilize phytoavailable P in biochar-based fertilizers with higher fertilizer effectiveness.

Entrapment of nano-ZnO into alginate/polyvinyl alcohol beads with different crosslinking ions for fertilizer applications.

Zinc oxide nanoparticles (nano-ZnO) are attractive as fertilizer materials but high concentrations may negatively affect the environment. To reduce their dispersion in the environment we entrapped nano-ZnO in biodegradable polymer beads consisting of alginate and polyvinyl alcohol (PVA). The alginate/PVA/ZnO beads were prepared via ionotropic gelation using two different crosslinking ions (Ca2+ and Zn2+), and the effect of alginate crosslinking ion and PVA content on bead structure, water absorption, water retention and zinc release was investigated. The pure CaAlg and ZnAlg beads demonstrated a poor water absorption and retention, which were strongly enhanced by the incorporation of PVA into the beads. The continuous Zn release was measured in a sand column, and it was found that the Zn-crosslinked beads rapidly released high concentrations of Zn followed by a more gradual Zn release, whereas Ca alginates showed only a gradual Zn release. The Zn dissolution kinetics could be tuned by the crosslinking ion composition. The prepared nano-ZnO-containing alginate/PVA beads may be attractive for Zn fertilizer applications under water-limited conditions.

Synthesis of nanocomposite hydrogel based carboxymethyl starch/polyvinyl alcohol/nanosilver for biomedical materials.

Treatment of infections using wound dressing integrated with multiple functions such as antibacterial activity, non-toxicity, and good mechanical properties has attracted much attention. In this study, carboxymethyl starch/polyvinyl alcohol/citric acid (CMS/PVA/CA) hydrogels containing silver nanoparticles (AgNPs) were prepared. The CMS, PVA and CA were used as polymer matrix and bio-based reducing agents for green synthesis of AgNPs. Silver nitrate (AgNO3) concentrations of 50, 100, and 150 mM were used to obtain nanocomposite hydrogels containing different AgNPs concentrations (AgNPs-50, AgNPs-100 and AgNPs-150, respectively). The minimum inhibitory concentration against E. coli and S. aureus was observed in CMS/PVA/CA hydrogels containing AgNPs-50. Uniform dispersion of AgNPs-100 in the hydrogel provided the highest storage modulus at 56.4 kPa. AgNPs-loaded hydrogels showed low toxicity to human fibroblast cells indicating good biocompatibility. Incorporation of AgNPs demonstrated an enhancement in antibacterial properties and overall mechanical properties, which makes these nanocomposite hydrogels attractive as novel wound dressing materials.

Lignin materials for adsorption: Current trend, perspectives and opportunities.

Lignin is a highly aromatic low value biomass residue, which can be utilized for chemicals, fuels and materials production. In recent years significant attention has focused on adsorbent materials from lignin. However, only 5% of available lignin is exploited worldwide, thus significant opportunities still exist for materials development. This review summarizes recent research advances in lignin-based adsorbents, with a particular emphasis on lignin, its modification and carbon materials derived from this abundant feedstock. Lignin derived activated carbons have been utilized for air pollutant adsorption (e.g. CO2, SO2 and H2S), while modified lignin materials have been developed for the removal of organic dyes and organics (like methylene blue, Procion Blue MX-R and phenols), heavy metals (such as Cu, Zn, Pb and Cd), or recovery of noble metals (e.g., Pd, Au and Pt). Future perspectives highlight how green chemistry approaches for developing lignin adsorbents can generate added value processes.